Sentence examples for apparent variant from inspiring English sources

Finally, there are no examples of human lymphoid malignancies (or any other type of malignancy) where the genome was altered by a RAG transpositional insertion of signal ends (or any other apparent variant of such a transposition).

Considering the highly stage-specific expression pattern of genes encoding exported proteins [ 2, 20], we wanted to determine whether the apparent variant expression pattern across patients' co-expression might be driven by differences in parasite life cycle stages between samples.

Neither yielded apparent variants at the initial stage of data analysis.

Apparent variants were removed if they also appeared in a pool of paired end sequences from 18 other unrelated samples from cancers, normal tissue or cell lines.

Fifty hours was the interval between receipt of a blood sample and identification of a provisional molecular diagnosis, provided that the diagnosis was readily apparent upon variant filtering.

The C→T substitution altered the predicted target site for MIR628 hsa-miR-628-3p hsa-miR-628-3p hsa-miR-628-3p hsa-miR-628-3ps < −0.1), suggesting that this "apparent silent" variant miRNAave an effect creating abinding ciscoreulatory element for miRNA (Table 1).

It is likely that a proportion of these sequence variants, including some missense mutations and apparent truncation variants such as G5199T [ 2], may exert a pathogenic effect by disrupting ESE motifs and altering BRCA1 splicing.

However, the majority of these apparent HLOF variants were likely to be second-generation sequencing errors, rare errors in the reference genome or variants that do not disrupt gene function.

As previously reported [ 31], most of these apparent P1 variants probably represent errors in TAIR9.

Errors produced by inaccurate mapping and the misalignment of short sequencing reads can create the appearance of apparent sequence variants that do not actually exist [ 14, 33].

SNPs predicted to have more than 2 alleles, or that mapped to an undetermined (N) base were excluded, as were SNP likely to be due to base calling errors close to homopolymer tracts and SNP calls resulting from apparent rare variants.